Interleukin-6 promotes arthritis and joint deformation in patients with systemic lupus erythematosus

被引:54
作者
Eilertsen, G. O. [2 ]
Nikolaisen, C. [2 ]
Becker-Merok, A. [2 ]
Nossent, J. C. [1 ,2 ]
机构
[1] Univ Hosp No Norway, Dept Rheumatol, N-9038 Tromso, Norway
[2] Univ Tromso, Inst Clin Med, Dept Rheumatol, N-9001 Tromso, Norway
关键词
arthritis; cytokines; systemic lupus erythematosus; CITRULLINATED PEPTIDE ANTIBODIES; JACCOUDS ARTHROPATHY; DISEASE-ACTIVITY; DEFORMING ARTHROPATHY; RHEUMATOID-ARTHRITIS; ALPHA BLOCKADE; TNF-ALPHA; CRP; EFFICACY; PLASMA;
D O I
10.1177/0961203310392432
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The underlying mechanisms for the subsets of self-limiting, intermittent or chronic and deforming arthritis in systemic lupus erythematosus (SLE) are not well understood. We performed a cross-sectional analysis of pro-inflammatory cytokines (IL-1 beta, IL-2, IL-6, IL-8 and TNF-alpha) and joint status in 47 SLE patients (79% females, age 42 years, disease duration 8.6 years). All cytokines levels were significantly elevated in SLE patients compared with controls, but only IL-2 and IL-8 levels were higher than in patients with rheumatoid arthritis. SLE patients with ongoing synovitis (19%) and joint deformities (11%) had increased erythrocyte sedimentation rate (ESR), IL-6 and anti-dsDNA Ab levels. IL-6 levels correlated with ESR, anti-dsDNA Ab and haemoglobin, but not with C-reactive protein levels. Arthritis constitutes a considerable burden of disease in SLE over time, and joint deformations are associated with longstanding disease and arthritis flare rates. IL-6 is a potential biomarker and therapeutic target in the prevention of joint damage in SLE arthritis. Lupus (2011) 20, 607-613.
引用
收藏
页码:607 / 613
页数:7
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